One-Step Conversion of Ketones to Conjugated Acids Using Bromoform
Само за регистроване кориснике
2009
Аутори
Vitnik, VesnaIvanović, M.D.
Vitnik, Željko J.
Popović-Djordjević, Jelena
Zizak, Z.S.
Juranić, Zorica
Juranić, Ivan O.
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
Phase-transfer-catalyzed (PTC) reactions of ketones with bromoform and aqueous lithium hydroxide in alcoholic solvent result in the formation of alpha,beta-unsaturated carboxylic acids. The reaction was performed at room temperature for 24h. The corresponding conjugated acids were obtained from cyclic or aromatic ketones, whereas bromo acids were obtained from 4-oxo-piperidine-1-carboxylic acid ethyl ester (13) and 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (14).
Кључне речи:
Bromoform / phase-transfer-catalyzed reaction / -unsaturated carboxylic acidsИзвор:
Synthetic Communications, 2009, 39, 8, 1457-1471Издавач:
- Taylor & Francis Inc, Philadelphia
Финансирање / пројекти:
- Нови синтетички приступи, молекулско моделовање и фармаколошко испитивање хетероцикличних система са азотом (RS-MESTD-MPN2006-2010-142074)
- Синтеза, карактеризација и активност органских и координационих једињења и њихова примена у (био)нанотехнологији (RS-MESTD-MPN2006-2010-142010)
DOI: 10.1080/00397910802531955
ISSN: 0039-7911
WoS: 000264343400014
Scopus: 2-s2.0-67650257390
Институција/група
Poljoprivredni fakultetTY - JOUR AU - Vitnik, Vesna AU - Ivanović, M.D. AU - Vitnik, Željko J. AU - Popović-Djordjević, Jelena AU - Zizak, Z.S. AU - Juranić, Zorica AU - Juranić, Ivan O. PY - 2009 UR - http://aspace.agrif.bg.ac.rs/handle/123456789/2112 AB - Phase-transfer-catalyzed (PTC) reactions of ketones with bromoform and aqueous lithium hydroxide in alcoholic solvent result in the formation of alpha,beta-unsaturated carboxylic acids. The reaction was performed at room temperature for 24h. The corresponding conjugated acids were obtained from cyclic or aromatic ketones, whereas bromo acids were obtained from 4-oxo-piperidine-1-carboxylic acid ethyl ester (13) and 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (14). PB - Taylor & Francis Inc, Philadelphia T2 - Synthetic Communications T1 - One-Step Conversion of Ketones to Conjugated Acids Using Bromoform EP - 1471 IS - 8 SP - 1457 VL - 39 DO - 10.1080/00397910802531955 ER -
@article{ author = "Vitnik, Vesna and Ivanović, M.D. and Vitnik, Željko J. and Popović-Djordjević, Jelena and Zizak, Z.S. and Juranić, Zorica and Juranić, Ivan O.", year = "2009", abstract = "Phase-transfer-catalyzed (PTC) reactions of ketones with bromoform and aqueous lithium hydroxide in alcoholic solvent result in the formation of alpha,beta-unsaturated carboxylic acids. The reaction was performed at room temperature for 24h. The corresponding conjugated acids were obtained from cyclic or aromatic ketones, whereas bromo acids were obtained from 4-oxo-piperidine-1-carboxylic acid ethyl ester (13) and 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (14).", publisher = "Taylor & Francis Inc, Philadelphia", journal = "Synthetic Communications", title = "One-Step Conversion of Ketones to Conjugated Acids Using Bromoform", pages = "1471-1457", number = "8", volume = "39", doi = "10.1080/00397910802531955" }
Vitnik, V., Ivanović, M.D., Vitnik, Ž. J., Popović-Djordjević, J., Zizak, Z.S., Juranić, Z.,& Juranić, I. O.. (2009). One-Step Conversion of Ketones to Conjugated Acids Using Bromoform. in Synthetic Communications Taylor & Francis Inc, Philadelphia., 39(8), 1457-1471. https://doi.org/10.1080/00397910802531955
Vitnik V, Ivanović M, Vitnik ŽJ, Popović-Djordjević J, Zizak Z, Juranić Z, Juranić IO. One-Step Conversion of Ketones to Conjugated Acids Using Bromoform. in Synthetic Communications. 2009;39(8):1457-1471. doi:10.1080/00397910802531955 .
Vitnik, Vesna, Ivanović, M.D., Vitnik, Željko J., Popović-Djordjević, Jelena, Zizak, Z.S., Juranić, Zorica, Juranić, Ivan O., "One-Step Conversion of Ketones to Conjugated Acids Using Bromoform" in Synthetic Communications, 39, no. 8 (2009):1457-1471, https://doi.org/10.1080/00397910802531955 . .